{{Rsnum
|rsid=104893611
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CFC1
|position=130597896
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CFC1
}}{{omim
|id=605194
|rsnum=104893611
|variant=0001
}}{{ClinVar
|rsid=104893611
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=131355469
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=CFC1:55997
|GENE_NAME=CFC1
|GENE_ID=55997
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.131355469G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605194.0001
|CLNSIG=5
|CLNCUI=C1854334
|CLNDBN=Heterotaxy, visceral, 2, autosomal
|Disease=Heterotaxy
|CLNACC=RCV000005496.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1854334:605376:450
}}